A Phase I Comparative Pharmacokinetic and Safety Study of Two Intravenous Formulations of Vinorelbine in Patients With Advanced Non-Small Cell Lung Cancer

被引:0
|
作者
Wu, Guolan [1 ,2 ]
Wu, Lihua [1 ,2 ]
Zhou, Huili [1 ,2 ]
Lin, Meihua [1 ,2 ]
Peng, Ling [3 ]
Wang, Yina [4 ]
Zhai, You [1 ,2 ]
Hu, Xingjiang [1 ,2 ]
Zheng, Yunliang [1 ,2 ]
Lv, Duo [1 ,2 ]
Liu, Jian [1 ,2 ]
Shentu, Jianzhong [1 ,2 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Res Ctr Clin Pharm,State Key Lab Diag & Treatment, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Zhejiang Prov Key Lab Drug Evaluat & Clin Res, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Radiat Oncol, Hangzhou, Zhejiang, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Oncol, Hangzhou, Zhejiang, Peoples R China
关键词
pharmacokinetics; bioavailability; safety; vinorelbine; non-small-cell lung cancer; ABSOLUTE BIOAVAILABILITY; 1ST-LINE TREATMENT; ORAL VINORELBINE; SINGLE-AGENT; DOCETAXEL; TRIAL; NSCLC; INHIBITORS; NIVOLUMAB; DRUG;
D O I
10.3389/fphar.2019.00774
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: The aim of this study was to compare the pharmacokinetics and safety between two vinorelbine formulations [a new oil-in-water emulsion formulation (ANX) versus a previously marketed solution formulation (Navelbine)] in Chinese patients with advanced non-small cell lung cancer (NSCLC). Method: This was a single-center, randomized, open-label study. Eligible patients aged 18-70 years who had histologically or cytologically confirmed NSCLC were enrolled. In cycle 1, the patients alternatively received the two formulations (30 mg/m(2), given as a 10-min infusion) with a 7-day interval. Samples for pharmacokinetic analysis were taken during cycle 1. For all subsequent 21-day cycles (maximum four cycles), ANX was administered on days 1 and day 8. Bioequivalence analysis was performed on C-max, AUC(last), and AUC(inf). The safety profiles and anti-tumor effects were also determined. Results: From March 2013 to January 2015, 24 patients were enrolled and 20 were eligible for pharmacokinetic evaluation. The 20 subjects in the pharmacokinetic analysis set had a median age of 61 years (range, 37-70 years), and 15 patients were male (75%). Mean vinorelbine C-max, values for ANX and Navelbine were 1,317.40 and 1,446.30 ng/mL, respectively. Corresponding AUC(last) values were 797.08 and 924.26 ng.h/mL, respectively. AUC(inf) values were 830.14 and 957.16 ng.h/mL, respectively. Treatment ratios of the geometric means were 90.00% (90% CI, 83.22-99.07%) for C-max, 86.92% (90% CI, 80.91-93.37%) for AUC(last), and 87.44% (90% CI, 82.08-93.16%) for AUC(inf). These results met the required 80-125% bioequivalence criteria. The most frequently reported adverse events after vinorelbine administration were neutropenia, leucopenia, neutropenic fever, and constipation. Conclusion: At therapeutic dosage levels, pharmacokinetic behavior and safety profiles were similar for both formulations.
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页数:8
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